再狭窄
血小板活化
医学
阿司匹林
药理学
血小板
经皮冠状动脉介入治疗
氯吡格雷
传统PCI
药品
心脏病学
分泌物
细胞内
副作用(计算机科学)
皂甙
冠状动脉疾病
作用机理
血小板聚集抑制剂
限制
内科学
炎症
血小板粘附
化学
血小板膜糖蛋白
抗血小板药物
信号转导
作者
Xueli Lei,Chunlei Lv,Y. Zhang,Zhiyu Li,Hao Shen,Li Zhu
摘要
Percutaneous coronary intervention (PCI) enables coronary revascularisation and restores haemodynamic stability but also carries risks of delayed complications including in-stent restenosis (ISR), a chronic progressive disease with endovascular damage after PCI, which compromises the long-term efficacy of PCI. Currently, the main treatment strategies for ISR include interventional and drug therapies. From the era of using aspirin as a single antiplatelet agent to the 'gold standard' era of dual antiplatelet therapy, the risk of ISR after PCI has been reduced. However, long-term use of antiplatelet drugs inevitably causes a series of side effects such as gastrointestinal mucosal damage and bleeding, which have become key limiting factors in clinical treatment. Saponin natural products have been used to mitigate ISR progression by targeting platelet dysfunction. Specifically, these compounds directly bind to platelet membrane receptors, block ligand-receptor interactions, inhibit the secretion of α-granule and dense-granule contents, regulate intracellular signalling pathways and platelet metabolism, inhibit release of inflammatory mediators, and suppress platelet aggregation. This article reviews the progresses on the application of the active components in saponin natural products to inhibit platelet activation in the development of ISR after PCI, aiming to provide a superior approach for the comprehensive treatment of ISR after PCI.
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